Results 11 to 20 of about 32,192 (76)

Klippel-Feil Sendromu ve Otolojik Bulgular [PDF]

open access: yes, 2013
Klippel-Feil sendromu ilk kez 1912 yılında birbirinden bağımsız olarak Maurice Klippel ve Andre Feil tarafından tanımlanmıştır. Kısa geniş boyun, inferior yerleşimli ense sa ccedil; ccedil;izgisi, azalmış boyun hareketleri ana bulgularıdır ...
Oran, Abdülkadir   +4 more
core   +2 more sources

Concurrent Klippel-Feil Anomaly, Tethering and Dermoid Cyst Misinterpreted as Pott disease: A Case Report [PDF]

open access: yes, 2014
Klippel-Feil syndrome (KFS) is characterized by the failure in segmentation of two or more vertebrae due to an abnormal division of the mesodermal somites and has been reported to be associated with cardiac and central nervous system anomalies. We report
V Shanthi   +3 more
core   +2 more sources

Tratamiento del síndrome de Klippel-Feil mediante acupuntura japonesa método Manaka y moxibustión [PDF]

open access: yes, 2018
En este artículo se presenta el caso clínico de un nin˜ o de 12 an˜ os de edad que tiene asimetría de los hombros (síndrome de Klippel-Feil) y que recibió tratamientos de acupuntura-moxibustión Japonesa.
Pacheco, Sofia   +3 more
core   +1 more source

Síndrome de Klippel Feil: A Propósito de Un Caso [PDF]

open access: yes, 2021
The Klippel-Feil Syndrome (KFS) was first described by Maurice Klippel and Andre Feil in 1912, in a 46-year-old tailor who was admitted for “lung congestion and urinary alterations”.
Mauricio La Torre, Robinson
core  

Pseudodystonic Posture Secondary to Klippel–Feil Syndrome and Diastematomyelia [PDF]

open access: yes, 2015
Background: Dystonic postures possess a great number of differential diagnoses.Phenomenology Shown: We describe a pseudodystonic posture in a 61‐year‐old woman with skeletal and extra‐skeletal abnormalities. Educational Value: Klippel–Feil syndrome
Martin Lopez-Vicchi   +5 more
core   +1 more source

Síndrome de Klippel-Feil en un lactante [PDF]

open access: yes, 2022
The case report of an 11 months infant is presented, who was referred to the Clinical Genetics Service of the Medical Genetics Provincial Center in Holguín province, due to facial dysmorphias associated with motor retardation, short neck and decreasing ...
González Anta, Ana María   +2 more
core   +1 more source

Schizophrenia associated with Klippel-Feil syndrome and flat foot

open access: yes, 1995
SummaryA 20 year-old patient presented with schizophrenia which was associated with Klippel-Feil syndrome and flat foot.
BA Kareem   +4 more
core   +1 more source

Anaesthetic challenges in a patient with Klippel–Feil syndrome scheduled for panendoscopy and biopsy [PDF]

open access: yes, 2018
Klippel–Feil syndrome is one of the congenital causes of difficult airway. It is characterised by a classic triad of a short neck, restricted cervical spine movement, and a low posterior hairline, which can pose a significant challenge to the ...
Chitnis, A, Enohumah, K.O.
core  

Klippel-Feil syndrome: a case report [PDF]

open access: yes, 2017
Klippel-Feil Syndrome (KFS) is defined as congenital fusion of two or more cervical vertebrae. The most common signs are short neck, low hairline at the back of head and restricted mobility of neck.
Gupta, Richa   +3 more
core  

Congenital Heart Disease in Children with Klippel – Feil Syndrome Presentation of Four Cases and a Review of the Curent Literature [PDF]

open access: yes, 2015
Introduction: First time described in 1912, from Maurice Klippel and Andre Feil independently, Klippel-Feil syndrome (synonyms: cervical vertebra fusion syndrome, Klippel-Feil deformity, Klippel-Feil sequence disorder) is a bone disorder characterised by
Bejiqi, Hana
core   +1 more source

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